Cyclic oligomers comprising m-phenylene isophthalamide and polymers thereof

ABSTRACT

Disclosed herein are cyclic oligomers comprising substituted or unsubstituted m-phenylene isophthalamide, complexes of these oligomers with selected metal salts, novel methods for their preparation, and polymerization of the cyclic oligomers to linear aramids. The aramids are useful, for example, as fibers for fire resistant clothing. Amino-functional cyclic oligomers may be reacted with polyfunctional acyl halides to produce polyamides.

This application is a divisional application of Ser. No. 08/664,898,filed Jun. 18, 1996 now U.S. Pat. No. 5,770,675, and claims the prioritybenefit of U.S. Provisional Application 60/000,402, filed Jun. 21, 1995.

FIELD OF THE INVENTION

Described herein are cyclic oligomers comprising substituted orunsubstituted m-phenylene isophthalamides, their preparation, theircomplexes with certain metals salts, and their polymerization tocorresponding linear polyamides.

TECHNICAL BACKGROUND

Cyclic oligomers with repeat units corresponding to condensationpolymers such as polyesters and polycarbonates are known. These cyclicoligomers can often be converted to their corresponding linear polymersby ring-opening polymerization. Cyclic oligomers of some aromatic amideshave been made.

Cyclic oligomers of (substituted) p-phenylene terephthalamide have beenprepared. See, for example, W. Memeger Jr., et al., Macromolecules, vol.26, p. 3476-3484 (1993) and Polym. Prepr., vol. 34, p. 71-72 (1993). Nocyclic meta-substituted aromatic amides are disclosed in this paper.

F. E. Elhadi, et al., Tetrahedron Lett., vol. 21, p. 4215-4218 (1980)reports the synthesis of N-substituted cyclic trimers of m-aminobenzoicacid. Cyclic oligomers of diamines and dicarboxylic acids are notmentioned.

T. L. Guggenheim, et al., Polymer Prepr., vol. 30, p. 138-139 (1989)report the attempted synthesis of the cyclic oligomer of m-phenyleneisophthalamide by a high dilution reaction procedure, but they report no"appreciable amount of cyclic formation".

Y. H. Kim, et al., Abstracts of the 35th IUPAC International Symposiumon Macromolecules, University of Akron, Jul. 11-15, 1994, report thesynthesis of a nitro-substituted cyclic oligomer of m-phenyleneisophthalamide. Also reported is a metal salt complex of this cyclicoligomer.

SUMMARY OF THE INVENTION

This invention concerns a cyclic oligomer of the formula ##STR1##wherein: n is an integer ranging from 3 to 12;

each of R¹, R², and R³ is independently hydrogen, halogen, hydrocarbylcontaining 1 to 6 carbon atoms, or nitro; and

each of R⁴, R⁵, and R⁶ is independently hydrogen, halogne, orhydrocarbyl containing 1 to 6 carbon atoms.

This invention also concerns a complex between a cyclic oligomer of theformula ##STR2## and a metal chloride, wherein said metal is selectedfrom the group consisting of calcium, barium, strontium and thetransition metals, wherein:

n is an integer ranging from 3 to 12;

each of R¹, R², and R³ is independently hydrogen, halogen, hydrocarbylcontaining 1 to 6 carbon atoms, or nitro; and

each of R⁴, R⁵, and R⁶ is indendently hydrogen, halogen, or hydrocarbylcontaining 1 to 6 carbon atoms.

Also described herein is a process for the preparation of a cyclicoligomer, comprising contacting a first solution of a compound of theformula ##STR3## with a second solution of a compound of the formula##STR4## wherein

X is halogen;

each of R¹, R², and R³ is independently hydrogen, halogen, hydrocarbylcontaining 1 to 6 carbon atoms, or nitro; and

each of R⁴, R⁵, and R⁶ is hydrogen, halogen, or hydrocarbyl containing 1to 6 carbon atoms;

wherein said contacting is done with agitation or mixing;

the concentration of (II) in said first solution is about 0.1 molar orless; and

the concentration of (III) in said second solution is about 0.1 molar orless.

This invention also includes a process for the polymerization of acyclic oligomer of m-phenylene isophthalamide, comprising contactingsaid cyclic oligomer with a base which is capable of removing an amidohydrogen atom from said cyclic oligomer. Suitably, the polymerization iscarried out at a temperature of about 150° C. to about 380° C. in aninert liquid medium.

Also disclosed herein is a polymer, which is a reaction product of acompound of the formula ##STR5## with a compound of the formula

    R.sup.13 (COX).sub.2                                       (V)

wherein

each R⁷, R⁸, R⁹, R¹⁰, R¹¹, and R¹² is independently amino or hydrogen;

R¹³ is hydrocarbylene, X is halogen, provided that:

a total of at least two of R⁷, R⁸, R⁹, R¹⁰, R¹¹, and R¹² are amino;

the molar ratio of (V):(IV) is at least about 1:1; and

the molar ratio of (V):(IV) is such that number of equivalents of COXgroups in the reaction does not substantially exceed the number of aminogroups.

BRIEF DESCRIPTION OF THE DRAWING

FIG. 1 is the structure of the CaCl₂ complex of compound (I) above,wherein n=3 and R¹, R², R³, R⁴, R⁵ and R⁶ are all hydrogen, based onX-ray crystallography (see Example 13 below).

DETAILS OF THE INVENTION

Disclosed herein are cyclic oligomers of the formula (I) above, whichare cyclic oligomers, analogous to a polyamide, comprising substitutedor unsubstituted m-phenylene isophthalamide. In compounds of formula(I), it is preferred that R¹, R², R³, R⁴, R⁵, and R⁶ are all hydrogen.In another preferred embodiment of formula (I), the groups R¹, R³, R⁴,R⁵, and R⁶ are all hydrogen, and R² is nitro. It is also preferred thatn is 3 (cyclic trimer). By hydrocarbyl herein is meant a univalentradical containing only carbon and hydrogen, preferably containing 1 to6 carbon atoms, more preferably 1 to 4.

These cyclic oligomers form complexes with certain metal salts. Such acomplex may be formed by mixing a cyclic oligomer with a solution of themetal salt in a solvent or, alternatively, by forming the cyclicoligomer in the presence of the metal salt. The complex may be convertedback to the (simple) cyclic oligomer and free metal salt by washing thecomplex with a solvent for the salt such as water. Mixtures of solventsmay also be used, and mixtures of the above mentioned and similarsolvents with water are preferred. The preferred complexes have the sameformula for the cyclic oligomer as in the preferred cyclic oligomers bythemselves (described above). Preferred metal salts are calcium chlorideand ferric chloride.

FIG. 1 shows the structure of a complex wherein n is 3, R¹, R², R³, R⁴,R⁵, and R⁶ are all hydrogen, and the metal salt is calcium chloride.

The cyclic oligomers described herein may be made by high dilutionreaction techniques known in the art as being particularly useful forproducing cyclic compounds. See, for instance, L. F. Feiser, et al.,Organic Chemistry, 3rd Ed., Reinhold Publishing Corp. New York, 1956, p.318-320, which is hereby incorporated by reference. Dilute solutions ofthe two reactants (II) and (III) are mixed with good agitation,preferably at rates such that, at any given time, the concentration of(II) and (III) are each relatively low and the molar amounts of (II) and(III) in the solution are approximately equal. This will usually meanthat the molar rate of addition of (II) and (III) to the process will beapproximately equal. Solutions of (II) and (III) may be simultaneouslyadded to a portion of the solvent with agitation, as illustratd byExamples 1-8 below. In another method, dilute solutions of (II) and(III) are directly mixed together with good agitation in an impingingflow mixing tee.

Preferred solvents for the synthesis of the cyclic oligomers are thosenormally used for the synthesis of aramids, such asN,N-dimethylformamide, N,N-dimethylacetamide, N-methylpyrrolidone, andhexamethylphosphoramide. Especially preferred are N-methylpyrrolidoneand N,N-dimethylacetamide. The concentration of (II) and (III) in thefirst and second solutions respectively are each about 0.1 molar orless, preferably each about 0.01 molar or less. The temperature at whichthe process is carried out is not critical, a range of -5° C. to about+50° C. being convenient, preferably about -5° C. to about +5° C.

According to the present process, it is preferred that R¹, R², R³, R⁴,R⁵, and R⁶ are all hydrogen, or that R¹, R³, R⁴, R⁵, and R⁶ are allhydrogen and R² is nitro.

In the process for forming the cyclic oligomers comprising m-phenyleneisophthalamide, it has been found helpful to include in the solution inwhich the cyclic oligomer is forming a metal salt, as defined above. Itis believed that the metal salt acts something like a "template" toincrease the yield of cyclic oligomer. The salts which are used andpreferred above for the metal salt complex of the cyclic oligomers arealso useful and preferred in the process for the synthesis of the cyclicoligomers. The initial products, when these salts are present, are thesalt complexes of the cyclic oligomers. As described above, they arereadily converted to the cyclic oligomers themselves.

The cyclic oligomers may be converted to the corresponding linearpolymers by contacting the cyclic oligomers with a base capable ofremoving an amido hydrogen atom from the cyclic oligomer (the "firstpolymerization"). By this is meant that the base is basic enough toremove the hydrogen atom from the group --CO--NH-- which is present inthe cyclic oligomer. Suitable bases include, for example, those having ahydride anion, as in sodium hydride, an amide anion, as in potassium orsodium amide, or an alkoxide, as in sodium methoxide. Alkali metalhydride and alkoxides are preferred bases. Only a catalytic amount ofbase need be used, about 15 molar percent or less based on the amount ofcyclic oligomer present. During polymerization, it is preferred that R¹,R², R³, R⁴, R⁵, and R⁶ are all hydrogen. In other words, the cyclicoligomer of m-phenylene isophthalamide is polymerized to formpoly(m-phenylene isophthalamide).

The first polymerization is carried out at a temperature of about 150 toabout 380° C., preferably about 150 to about 300° C. It is suitablycarried out in an inert liquid medium, which may or may not dissolve thecyclic oligomer and/or basic catalyst. Suitable inert liquid mediainclude N,N-dimethylformamide, N,N-dimethylacetamide,N-methylpyrrolidone, diphenyl sulfone, tetramethylenesulfone, and thelike, wherein N-methylpyrrolidone and diphenyl sulfone are preferred. Inorder to avoid undesired side reactions, particularly of the basepresent, it is preferred that the process be carried out under an inertgas such as nitrogen or argon, and that the starting materials bereasonably dry.

The product of the first polymerization, poly(m-phenyleneisophthalamide), and its substituted analogs, are aramids which areuseful for making fire resistant garments, particularly of use tofirefighters. The cyclic oligomer may also be used to sequester certainmetal salts or to remove them from waste streams. The cyclic oligomersare also useful as a high temperature additive for polymers. The metalsalt complexes may be used as source of the metal salts, as when usedfor melting ice.

In a second polymerization, an amino functional cyclic amide (IV), asdefined above, is reacted with a difunctional acyl halide (V), as alsodefined above. When only two of R⁷, R⁸, R⁹, R¹⁰, R¹¹, and R¹² are amino,a linear polyamide is produced wherein the cyclic amide moieties derivedfrom (IV) alternates with the moieties derived from (V). When more thantwo of R⁷, R⁸, R⁹, R¹⁰, R¹¹, and R¹² are amino, a crosslinked thermosetpolymer will be produced if most of the amino groups are reacted withacyl halide groups. In the second polymerization, it is preferred thatR⁷, R⁹, and R¹¹, the substitutents on the ring derived from the diacid,are amino, and/or all of R⁸, R¹⁰, and R¹², the substituents on the ringderived from the diamine, are all hydrogen. It is also prefered that Xis chlorine and that a sufficient amount of (V) is added so that atleast 75 mole percent of the amino groups present are reacted. If athermoplastic, the polymer may be used as a molding resin. If it is notthermoplastic and/or crosslinked, it may be used as a thermoset resin.In both cases, parts for electrical equipment, especially useful at hightemperature, may be made.

In the Examples, the following abbreviations are used:

DMAc--N,N-dimethylacetamide

DMF--N,N-dimethylformamide

I--isophthalic

ICl--isophthaloyl chloride

MPD--m-phenylenediamine

NMP--N-methylpyrrolidone

NMR--nuclear magnetic resonance spectroscopy

EXAMPLE 1 Preparation of a Cyclic Trimer Complex

Isophthaloyl chloride (10.2 g) and 5.4 g of m-phenylenediamine weredissolved in 50 mL each of toluene and DMAc, respectively. Thesesolution were slowly added with agitation to 200 mL of DMAc containing5.55 g of CaCl₂ in a 500 mL three neck round bottom flask which iscooled by a ice bath. Total addition took 60 min. The solution wasstirred for two more hours, then poured to a mixture of 200 mL ofmethanol and 100 mL water. The precipitate was washed and dried at 100°C. under vacuum to give 11.25 g of crude product. This solid wasrecrystallized from 50 mL DMAc containing 5.5 g of CaCl₂ and 2 mL water,to give 2.31 g of product, which is found to be a pure complex of cyclictrimer and CaCl₂.

In a separate experiment, the reaction mixture was neutralized withCa(OH)₂ with similar results.

EXAMPLES 2-3 Preparation of Cyclic Trimer and Complex

Examples 2-4 were run in a similar way to Example 1. Results are in theTable below.

    ______________________________________                                                                         DMAc  Weight of                                              Salt weight                                                                             [salt] Solvent                                                                             Complexed                              Example                                                                              Salt     (g)       [Amide]                                                                              (ml)  Crystal                                ______________________________________                                        2      No salt  NA        NA     300   0.57                                   3      CaCl.sub.2                                                                             5.55      1.0    300   0.27                                   ______________________________________                                    

* All experiments were conducted with 10.15 g of ICI in 70 mL tolueneand 5.40 g of MPD in 70 mL DMAc solvent, otherwise as the proceduredescribed in Example 1.

EXAMPLES 4-8 Preparaton of Cyclic Trimer and Complex

The procedure described in Example 1 was repeated, except NMP was usedas the solvent. Results are shown in the Table below.

    ______________________________________                                                                         NMP   Weight of                                              Salt weight                                                                             [salt] Solvent                                                                             Complexed                              Example                                                                              Salt     (g)       [Amide]                                                                              (ml)  Crystal                                ______________________________________                                        4      No salt  NA        NA     300   1.395                                  5      CaCl.sub.2                                                                             2.78      0.5    300   1.354                                  6      CaCl.sub.2                                                                             8.32      1.5    300   1.922                                  7      CaCl.sub.2                                                                             5.55      1.0    100   0.584                                  8      FeCl.sub.3                                                                             8.11      1.0    300   5.305                                  ______________________________________                                    

* All experiments were conducted with 10.15 g of ICI in 50 mL tolueneand 5.40 g of MPD in 50 mL NMP solvent, otherwise as the proceduredescribed in Example 1.

EXAMPLE 9 Ring Opening Polymerization of MPD-I Cyclic Trimer

To 4.6 mL of NMP containing 0.002 g of sodium hydride (0.083 mmol) wasadded the cyclic trimer (0.450 g, 0.63 mmol), which caused evolution ofgas, then heated to 100° C. The mixture was opaque with a slight yellowcolor. After 30 min, 0.0097 g of N-acetyl-epsilon-caprolactam (0.063mmol) in 0.5 mL of NMP was added, and then the temperature was set for210° C. After about 2 hours, a small layer of translucent liquid wasobserved above an opaque off-white mixture below which exhibited aslight increased viscosity. After 4 hours, when the reaction mixtureconsisted of a well dispersed white solid in the solvent, it was allowedto cool to RT (room temperature) and filtered, then washed with waterand finally dried in a vacuum oven at 100° C. Total 0.42 g of polymerwith 0.104 dL/g inherent viscosity (0.5 wt % at 30° C. in 98.5% H2SO₄)was obtained.

EXAMPLE 10 Ring Opening Polymerization of MPD-I Cyclic Trimer

To 4.1 g of phenylsulfone containing 0.002 g of sodium hydride (0.083mmol) was added the cyclic trimer (0.448 g, 0.63 mmol), then heated to150° C., where the solvent melted and gas was evolved. The mixtureturned opaque within 1 hour. The vessel was cooled to room temperature,and 0.0097 g of N-acetyl-epsilon-caprolactam (0.063 mmol) in 0.5 mL ofphenyl sulfone was added. Then the mixtureit was slowly heated to 265°C. for one hour. The solid was transferred to an Erlenmeyer flask aftercooling, and washed with hot MeOH to remove the phenyl sulfone then withhot water. The polymer was obtained by filtration, followed by vacuumdrying at 100° C. in a vacuum oven. Total 0.42 g of polymer with 0.17dL/g inherent viscosity (0.5 wt % at 30° C. in 98.5% H₂ SO₄) wasobtained.

EXAMPLE 11 Dissolution of CaCl₂ from the Cyclic Complex

A CaCl₂ complex (100 mg) of a cyclic CaCl₂ complex obtained by theprocedure described in Examples 1-8 was treated with copious amount ofdeionized water overnight to give 51 mg of light tan colored material. ANMR analysis indicated that the it has lost about 50% of complexedCaCl₂.

EXAMPLE 12 Dissolution of CaCl₂ from the Cyclic Complex

CaCl₂ can be completely washed out from the complex prepared by theprocedure described in Examples 1-8. The CaCl₂ complex of a cyclicproduct was first treated with DMF, then washed with 3N HCl for 10-15minutes three times, followed by three times washing a mixture of DMFand water. An elemental analysis detected no chlorine.

EXAMPLE 13 Recrystallization of R² ═NO₂ Cyclic CaCl₂ Complex

A crude cyclization product of R² ═NO₂, which was obtained by a methodsimilar to that described in Example 1, was repeatedly precipitated intowater from a DMAc solution. This product (44 mg) was dissolved in 4.0 gof DMF containing 27 mg of CaCl₂, and then the flask was placed in aclosed chamber containing THF at the bottom. Single crystals suitablefor X-ray were formed in 3-4 days. The x-ray structure showed that twocyclic trimers are stacked each other with respect to each other 60° outof plane, and a CaCl₆ ⁻⁴ ion is complexed inside of the pocket of thecyclic compounds through hydrogen bonding between chloride and amidehydrogen.

A cyclic compound with R² ═H, as obtained from Example 3, was alsocrystallized similarly for x-ray crystallography. The crystal is atriclinic, belongs to P-1 space group with cell parameters of a=12.498,b=22.729, c=12.342 Å, α=99.457, β=105.796, γ=75.345°. Its structure isshown in FIG. 1. In this case the complex is formed between CaCl₃ ⁻ andthe cyclic compound. Two cyclic compounds are linked each other througha Ca(DMF)₆ ²⁺ ion.

EXAMPLE 14 Mass Spectroscopic Analysis of Crude Cyclization Product

The crude reaction products prepared by methods similar to those ofExamples 1 and 2 were compared using laser description ionization/timeof flight (IDL-TOF) mass spectroscopy, by dissolving the mixture in thedimethylsufoxide and 2-(4-hydroxyphenolazo)-benzoic acid (HABA) matrix.It showed that the relative concentration of cyclic trimer gets higherwhen CaCl₂ was present in the reaction media.

EXAMPLE 15 Preparation of Nitro-Substituted Cyclic Oligomer

To a 2-L 3-necked round bottom Morton type flask equipped with amechanically driven stirrer, N₂ line, and two 2500 mL dropping funnelswith side return loops was added 700 mL DMAc (dried over molecularsieves). Metaphenylene diamine (MPD) (10.81 g) in 100 mL DMAc and5-nitroisophthaloyl chloride (24.80 g) in toluene (100 mL) were placedin the separate dropping funnels and added to the cold (ice bath)reaction flask over a period of about 4.5 hours. During the addition,the reaction mixture remained clear. The mixture was then allowed tostand for 2 days, then poured into 750 mL MeOH and 250 mL H₂ O containedin an Erlenmeyer flask. The fine pale yellow ppt. which separated wasstirred for 2 hours, then filtered by suction through a fine fritteddisc Buchner funnel. Filtration required overnight, leaving a gelatinoussolvent-laden filter cake. This was washed further by slurrying withMeOH, filtered, then dried overnight in 95 vacuum oven. Upon removalfrom oven, it was noticed that some soft viscous material was present inthe solids. The material was subsequently washed further with MeOH in ablender and filtered by suction and dried at 95° C./vac. oven. The yieldwas 14.1 g.

To 50.5 mL DMAc in 250 mL 3-necked round bottom flask with condenserdrying tube and N₂ line was added 5.3 g dry CaCl₂. Upon heating to 150°C. in an oil bath, the CaCl₂ did not completely dissolve. The aboveproduct (13.6 g) was added and after heating for 2 days at 160° C., aslightly viscous slurry was obtained. DMAc (50 mL) was added and afterabout 1 hour a clear solution was obtained. About 30 mL of the DMAc wasremoved and the solution began to cloud. The mixture was allowed to cooland stand overnight at RT whereupon 1.5 cc water was added whichappeared to precipitate additional solid. The solid was filtered on afine fritted disk Buckner funnel, washed with cold DMAc, and sucked dryunder N₂ overnight. The white powder (3.7 g) was transferred to a bottleand dried at 100° C. in a vacuum oven. The yield was 3.6 g. Another 0.4g of product crystallized from the filtrate. The combined material (3.96g) was boiled in 40 mL water for 2.5 hours, then filtered by suction,and then washed free of chloride with boiling water. The off-white solidwas dried overnight in a 100° C. vacuum oven. The yield was 2.67 g, and0.20 g of product was recrystallized from 15 mL DMAc. This was done bydissolving in DMAc and seeding with the crude product, followed bycooling in dry ice/acetone until the DMAc began to freeze. Afterstanding at RT for 5 days, the crystals were collected by suctionfiltrate, then dried at 110° C. under vaccuum in an oven. The yield was0.11 g. The remainder of the product was recrystallized in a similarfashion. The FAB MS of the product exhibited a peak at M+H=849.67corresponding to the cyclic trimer.

EXAMPLE 16 Preparation of Amine-Substituted Cyclic Oligomer

To 150 mL of DMAc was added 0.1 g of 5% Pd on charcoal and to thismixture was added 2.0 g of the nitro-substituted cyclic oligomer (seeabove for preparation). The mixture was treated with H₂ at 100° C. under130 psi for 4 hours. The catalyst and charcoal were removed byfiltration and the product recovered as a solid by rotary evaporation ofthe DMAc. The FAB MS of the product exhibited a peak at M+H=759.94corresponding to the amine substituted cyclic trimer.

EXAMPLE 17 Preparation of Polyamide-Containing Cyclic Oligomers ofm-Phenyleneisophthalamide

To 0.55 g of CaCl₂ in 200 mL cylindrical round bottom flask with N₂ lineand 316-stainless steel basket stirrer was added 24.3 g of NMP and afterstirring for 5 minutes, 1.25 g of the above crude amine substitutedcyclic trimer was added. About 2.5 mL of NMP was used as a wash toremove the cyclic trimer from the sides of the flask but was notcompletely effective. A spatula was then used to scrape the materialfrom the walls. The system was then heated to 70° C. whereupon a clearbrown solution was obtained. The mixture was cooled in an ice bath for20 minutes, and then 0.60 g terephthaloyl chloride was added all atonce. The mixture gave a clear yellow gel within a few seconds, which,after a short time (minutes), fractured fairly easily. After 45 minutes,0.092 g of CaCl₂ was added and stirring continued for 20 minutes more.No significant change occurred in consistency of the gel. Examinationunder crossed optical polarizers revealed only minor birefringence. Uponshearing, the degree of birefringence increased. NMP (5 mL) was added,stirring was continued for 5 minutes, and then another 3 mL NMP wasadded. The gel softened over the next 20 minutes whereupon 0.24 g CaCl₂was added. After another hour, the gel exhibited appreciable flow (gelflowed away from the wall when the stirrer was stopped). More NMP (3 mL)was added and stirring continued (elapsed time 3.5 hours). After anotherhour, the moderately viscous mixture containing undissolved gel particlewas heated to 50° C. and held overnight. After standing for severaldays, an aliquot (21 mL) of the mixture was centrifuged using a heated(50° C.) centrifuge. The nearly clear greenish upper layer was removedwith a syringe and transferred to a glass plate, covering an area ofabout 4 in.×3 in. After drying overnight in a 60° C. vacuum oven andthen standing under N₂ in an oven for 3 days, the film was surprisinglycoherent and released easily when a razor blade was inserted between thefilm and glass. Several small strips were removed and soaked indistilled water for several hours. Pieces of the coherent films weredried between paper towels and on glassine paper, respectively, in a 90°C. vacuum oven. The uncentrifuged remainder of the mixture wasprecipitated by addition of water filtered by suction, and then washedtwice with hot water by magnetically stirring on a hot plate. The solidwas finally washed with hot 2B alcohol and dried in a 90° C. vac. oven.The product exhibited an η_(inh) of 0.47 (conc. of 0.50 w/v % in conc.H₂ SO₄ at 30° C.). Further, the polymer exhibited outstanding thermalstability with a TGA decomposition temperature of 400° C. in N₂ (heatingrate -20° C./min.), but with 95% weight retention at 500° C.

What is claimed is:
 1. A polymer, which is a reaction product of acompound of the formula ##STR6## with a compound of the formula

    R.sup.13 (COX).sub.2                                       (V)

wherein each R⁷, R⁸, R⁹, R¹⁰, R¹¹, and R¹² is independently amino orhydrogen; R¹³ is hydrocarbylene, X is halogen, provided that: a total ofat least two of R⁷, R⁸, R⁹, R¹⁰, R¹¹, and R¹² are amino; the molar ratioof (V):(IV) is at least about 1:1; and the molar ratio of (V):(IV) issuch that number of equivalents of COX groups in the reaction does notsubstantially exceed the number of amino groups.
 2. The polymer asrecited in claim 1 wherein X is chlorine, all of R⁷, R⁹, and R¹¹ areamino, and all of R⁸, R¹⁰ and R¹² are hydrogen.